Canonical Allele Identifier: CA1619763311

Gene: TAP1 PSMB9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32848597_32848598delinsAG , CM000668.2:g.32848597_32848598delinsAG	GRCh38
NC_000006.11:g.32816374_32816375delinsAG , CM000668.1:g.32816374_32816375delinsAG	GRCh37
NC_000006.10:g.32924352_32924353delinsAG	NCBI36
NG_011759.1:g.10374_10375delinsCT
NG_028165.1:g.1338_1339delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*718+54_*718+55delinsCT (TAP1)	ENSP00000513708.1:n.*718+54_*718+55delinsCT
ENST00000698421.1:c.*460+54_*460+55delinsCT (TAP1)	ENSP00000513709.1:n.*460+54_*460+55delinsCT
ENST00000698422.1:c.1377+392_1377+393delinsCT (TAP1)	ENSP00000513710.1:n.1377+392_1377+393delinsCT
ENST00000698423.1:c.1566+54_1566+55delinsCT (TAP1)	ENSP00000513711.1:n.1566+54_1566+55delinsCT
ENST00000698424.1:c.1437+54_1437+55delinsCT (TAP1)	ENSP00000513712.1:n.1437+54_1437+55delinsCT
ENST00000354258.5:c.1566+54_1566+55delinsCT (TAP1) MANE Select	ENSP00000346206.5:n.1566+54_1566+55delinsCT
ENST00000643049.2:c.142-536_142-535delinsCT (TAP1)	ENSP00000494148.2:n.142-536_142-535delinsCT
ENST00000643923.1:n.1002+54_1002+55delinsCT (TAP1)
ENST00000645078.1:n.1161+54_1161+55delinsCT (TAP1)
ENST00000354258.4:c.1746+54_1746+55delinsCT (TAP1)	ENSP00000346206.4:n.1746+54_1746+55delinsCT
ENST00000395330.5:c.-10+4323_-10+4324delinsAG (PSMB9)	ENSP00000378739.1:n.-10+4323_-10+4324delinsAG
ENST00000414474.5:c.-10+3727_-10+3728delinsAG (PSMB9)	ENSP00000394363.1:n.-10+3727_-10+3728delinsAG
ENST00000486332.1:n.1491+54_1491+55delinsCT (TAP1)
NM_000593.5:c.1746+54_1746+55delinsCT (TAP1)	NP_000584.2:n.1746+54_1746+55delinsCT
NM_001292022.1:c.963+54_963+55delinsCT (TAP1)	NP_001278951.1:n.963+54_963+55delinsCT
NM_001292022.2:c.963+54_963+55delinsCT (TAP1)	NP_001278951.1:n.963+54_963+55delinsCT
NM_000593.6:c.1566+54_1566+55delinsCT (TAP1) MANE Select	NP_000584.3:n.1566+54_1566+55delinsCT